在一种遗传性肥胖的小鼠模型中,达到体重峰值的年龄与寿命相关。

The age of attaining highest body weight correlates with lifespan in a genetically obese mouse model.

机构信息

Division of Breeding Biology and Molecular Genetics, Department of Crop and Animal Sciences, Humboldt-Universität zu Berlin, Berlin, Germany.

出版信息

Nutr Diabetes. 2013 Mar 18;3(3):e62. doi: 10.1038/nutd.2013.4.

Abstract

Obesity has been associated with a higher risk of mortality, whereas caloric restriction reduces the risk. In this study, we examined how body weight development during life affects lifespan in a mouse model for obesity. Therefore, mice of the Berlin Fat Mouse Inbred line were set on either a standard or a high-fat diet (HFD). Median lifespans of standard diet-fed mice were 525 and 539 days for males and female animals, respectively. HFD feeding further decreased lifespan by increasing the risk of mortality. Our data provide evidence that the highest body weight reached in lifetime has only a minor effect on lifespan. More important is the age when the highest body weight is reached, which was positively correlated with lifespan (r=0.77, P<0.0001). Likewise, the daily gain of body weight was negatively correlated with the age of death (r=-0.76, P<0.0001). These data indicate that rapid weight gain in early life followed by rapid weight loss affect lifespan more than the body weight itself. These data suggest that intervention strategies to prevent rapid weight gain are of high impact for a long lifespan.

摘要

肥胖与更高的死亡率相关,而热量限制则降低了这种风险。在这项研究中,我们研究了肥胖小鼠模型中生命过程中的体重变化如何影响寿命。为此,我们将柏林肥胖小鼠近交系的小鼠置于标准饮食或高脂肪饮食(HFD)中。标准饮食喂养的雄性和雌性小鼠的中位寿命分别为 525 天和 539 天。HFD 喂养进一步通过增加死亡率风险而降低了寿命。我们的数据提供了证据,表明一生中达到的最高体重对寿命只有较小的影响。更重要的是达到最高体重的年龄,这与寿命呈正相关(r=0.77,P<0.0001)。同样,体重的日增重与死亡年龄呈负相关(r=-0.76,P<0.0001)。这些数据表明,生命早期的快速体重增加随后快速体重减轻比体重本身对寿命的影响更大。这些数据表明,预防快速体重增加的干预策略对长寿具有重要影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f79f/3608894/2fb85c6dbd46/nutd20134f1.jpg

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